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Journal of Energy Chemistry 2013, Vol. 22 Issue (1) :1-20    DOI:
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Recent progress in methane dehydroaromatization: From laboratory curiosities to promising technology

Shuqi Maa,b, Xiaoguang Guoa, Lingxiao Zhaoa, Susannah Scottc, Xinhe Baoa*
a. State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, the Chinese Academy of Sciences, Dalian 116023, Liaoning, China; b. School of Physics

and Chemistry, Henan Polytechnic University, Jiaozuo 454000, Henan, China; c. Department of Chemistry & Biochemistry, and Department of Chemical

Engineering, University of California, Santa Barbara, California 93106, United States


Abstract

 Direct conversion of methane to benzene or other valuable chemicals is a very promising process for the efficient application of natural gas. Compared with conversion processes that require oxidants, non-oxidative direct conversion is more attractive due to high selectivity to the target product. In this paper, an alternative route for methane dehydrogenation and selective conversion to benzene and hydrogen without the participation of oxygen is discussed. A brief review of the catalysts used in methane dehydroaromatization (MDA) is first given, followed by our current understanding of the location and the active phase of Mo species, the reaction mechanism, the mechanism of carbonaceous deposit and the deactivation of Mo/zeolite catalysts are systematically discussed. Ways to improve the catalytic activity and stability are described in detail based on catalyst and reaction as well as reactor design. Future prospects for methane dehydroaromatization process are also presented.
Keywords: direct conversion methane methane dehydroaromatization Mo-based catalyst   
Received: 2013-01-07; published: 2013-02-06
Cite this article:   
Shuqi Ma, Xiaoguang Guo, Lingxiao Zhao etc .Recent progress in methane dehydroaromatization: From laboratory curiosities to promising technology [J]  Journal of Energy Chemistry, 2013,V22(1): 1-20
URL:  
http://www.jenergchem.org/EN/     或     http://www.jenergchem.org/EN/Y2013/V22/I1/1
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